FDA Inspection
Ajinomoto Althea, Inc.Ajinomoto Althea, Inc. – FDA Inspection, Mar 22, 2019
Record Details
This FDA Inspection record concerns Ajinomoto Althea, Inc., with an inspection on March 22, 2019, issued by the Los Angeles District Office, covering human drugs.
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ID · a29e693e-d817-47b5-ab56-bf57f9a19305
Inspection Facts
- Inspection number
- 1088015
- FDA center
- Human Drugs
- Outcome
- Form 483 issued
Other FDA inspections of Ajinomoto Althea, Inc.
16| Date | Classification | Office | Project area |
|---|---|---|---|
| May 9, 2025 | VAI | Los Angeles District Office | Drug Quality Assurance |
| September 20, 2023 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| February 9, 2023 | Not classified | Los Angeles District Office | |
| January 16, 2023 | Not classified | Los Angeles District Office | |
| May 25, 2021 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
Other documents for Ajinomoto Althea, Inc.
- FDA Inspection 1266794 - 2025-05-09
- FDA Inspection 1218719 - 2023-09-20
- FDA Inspection 1223371 - 2023-02-09
- FDA Inspection 1195170 - 2023-01-16
- FDA Inspection 1142663 - 2021-05-25
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